TABLE 4.

SNPs and effect alleles within SLC44A1 showing an association with FASD or are in linkage-disequilibrium with these SNPs¹

SNP	Nucleotide	Location	Effect allele (major > minor allele in dbSNP)2
rs327959	105,246,149	Intron 1	Increased with T (C > T)
rs327956	105,246,635	Intron 1	Increased with A (G > A)
rs443094	105,254,404	Intron 1	Increased with C (G > C)
rs328006	105,277,527	Intron 1	Increased with C (G > C)
rs327947	105,280,309	Intron 1	Increased with G (A > G)
rs193008	105,280,525	Intron 1	Increased with C (T > C)
rs12335779	105,288,137	Intron 1	Increased with G (C > G)
rs10991611	105,301,414	Intron 2	Increased with T (C > T)
rs9644967	105,305,895	Intron 2	Increased with A (G > A)
rs10991618	105,310,238	Intron 3	Increased with A (G > A)
rs2417615	105,325,570	Intron 3	Increased with A (G > A)
rs6479311	105,347,335	Intron 4	Increased with A (C > A)
rs10991639	105,355,290	Intron 5	Increased with A (G > A)
rs7024985	105,358,537	Intron 7	Increased with T (C > T)
rs7865985	105,358,537	Intron 7	Increased with C (T > C)
rs10123494	105,359,416	Intron 7	Increased with C (T > C)
rs34750132	105,360,429	Intron 7	Increased with G (A > G)
rs6479313	105,364,024	Intron 9	Increased with G (C > G)
rs7029443	105,367,465	Intron 12	Increased with A (T > A)
rs10820801	105,367,540	Intron 12	Increased with G (A > G)
rs4549843	105,368,325	Intron 12	Increased with A (G > A)
rs35603631	105,380,371	Intron 13	Increased with C (T > C)
rs16924529	105,382,872	Intron 13	Increased with A (G > A)
rs3199966	105,385,482	Exon 15	Increased with G (T > G)
rs12339823	105,387,394	Intron E15–E16	Increased with G (A > G)
rs2771040	105,389,918	Exon 16 3′-UTR	Increased with G (A > G)

¹E, exon; SNP, single nucleotide polymorphism; 3′-UTR, 3′-untranslated region.

²Measured on top strand 5′ → 3′. All of these alleles are single nucleotide variants.